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Human serum albumin as a clinically accepted cell carrier solution for skin regenerative application
The rules governing Medicinal Products in the European Union necessitates the production of cell-based therapy in good manufacturing practice facilities. The produced cells may need several hours in transportation to reach the application sites. In this study, we investigated four candidate solution...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468270/ https://www.ncbi.nlm.nih.gov/pubmed/32879384 http://dx.doi.org/10.1038/s41598-020-71553-2 |
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author | Shahin, Hady Elmasry, Moustafa Steinvall, Ingrid Markland, Katrin Blomberg, Pontus Sjöberg, Folke El-Serafi, Ahmed T. |
author_facet | Shahin, Hady Elmasry, Moustafa Steinvall, Ingrid Markland, Katrin Blomberg, Pontus Sjöberg, Folke El-Serafi, Ahmed T. |
author_sort | Shahin, Hady |
collection | PubMed |
description | The rules governing Medicinal Products in the European Union necessitates the production of cell-based therapy in good manufacturing practice facilities. The produced cells may need several hours in transportation to reach the application sites. In this study, we investigated four candidate solutions for transporting human keratinocytes. The solutions are (1) normal saline, (2) saline with 2.5% human serum albumin (Saline + HSA), (3) chemically defined, xeno-free keratinocyte media and (4) keratinocyte media with pituitary bovine extract (PBE-media). One million keratinocytes from three donors were suspended in each solution and kept at 4 °C for up to 24 h. Cells kept in Saline + HSA showed higher viability after 1, 3 and 24 h. Then, equal number of viable cells were seeded on collagenous matrix and cultured for 48 h. The adhesion and colonization were higher in the cells kept in PBE-media, while the keratinocyte surface marker, cytokeratin 14, was present in all studied groups. These results confirmed the suitability of Saline + HSA as a cell transportation solution for clinical use, which will be the choice for the planned clinical trial. Keratinocyte PBE-media can be an alternative for cells transported for research purpose, if the same media type is going to be used in the following experiments. |
format | Online Article Text |
id | pubmed-7468270 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74682702020-09-04 Human serum albumin as a clinically accepted cell carrier solution for skin regenerative application Shahin, Hady Elmasry, Moustafa Steinvall, Ingrid Markland, Katrin Blomberg, Pontus Sjöberg, Folke El-Serafi, Ahmed T. Sci Rep Article The rules governing Medicinal Products in the European Union necessitates the production of cell-based therapy in good manufacturing practice facilities. The produced cells may need several hours in transportation to reach the application sites. In this study, we investigated four candidate solutions for transporting human keratinocytes. The solutions are (1) normal saline, (2) saline with 2.5% human serum albumin (Saline + HSA), (3) chemically defined, xeno-free keratinocyte media and (4) keratinocyte media with pituitary bovine extract (PBE-media). One million keratinocytes from three donors were suspended in each solution and kept at 4 °C for up to 24 h. Cells kept in Saline + HSA showed higher viability after 1, 3 and 24 h. Then, equal number of viable cells were seeded on collagenous matrix and cultured for 48 h. The adhesion and colonization were higher in the cells kept in PBE-media, while the keratinocyte surface marker, cytokeratin 14, was present in all studied groups. These results confirmed the suitability of Saline + HSA as a cell transportation solution for clinical use, which will be the choice for the planned clinical trial. Keratinocyte PBE-media can be an alternative for cells transported for research purpose, if the same media type is going to be used in the following experiments. Nature Publishing Group UK 2020-09-02 /pmc/articles/PMC7468270/ /pubmed/32879384 http://dx.doi.org/10.1038/s41598-020-71553-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Shahin, Hady Elmasry, Moustafa Steinvall, Ingrid Markland, Katrin Blomberg, Pontus Sjöberg, Folke El-Serafi, Ahmed T. Human serum albumin as a clinically accepted cell carrier solution for skin regenerative application |
title | Human serum albumin as a clinically accepted cell carrier solution for skin regenerative application |
title_full | Human serum albumin as a clinically accepted cell carrier solution for skin regenerative application |
title_fullStr | Human serum albumin as a clinically accepted cell carrier solution for skin regenerative application |
title_full_unstemmed | Human serum albumin as a clinically accepted cell carrier solution for skin regenerative application |
title_short | Human serum albumin as a clinically accepted cell carrier solution for skin regenerative application |
title_sort | human serum albumin as a clinically accepted cell carrier solution for skin regenerative application |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468270/ https://www.ncbi.nlm.nih.gov/pubmed/32879384 http://dx.doi.org/10.1038/s41598-020-71553-2 |
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